23 results · 28ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

IMPLANT CENTER

FDA 510(k)
FDA Class 2 ·Dental

Vial Adaptor

FDA UDI
WEST PHARMA. SERVICES IL, . LTD·07290108240214·VA 20mm FLL TG- VF for J&J

Cook

FDA UDI
COOK INCORPORATED·00827002148611·Fascial Dilator

Glucose Standard (100 mg/dL)

FDA UDI
STANBIO LABORATORY, L.P.·00657498001165·For the Quantitative Determination of Glucose i...

Mick Vienna Needle Collector, 30ø

FDA UDI
MICK RADIO NUCLEAR INSTRUMENT, INC·00817330021649·

Tru-Paque

FDA UDI
Taub Products·D8370720300·Masks out metal partial framework, veneers, cop...

Arsenal

FDA UDI
ALPHATEC SPINE, INC.·00844856085534·SACRAL POLYAXIAL SCREW, 7.2mm X 30mm

Arsenal

FDA UDI
ALPHATEC SPINE, INC.·00844856084384·POLYAXIAL SCREW, 7.2mm X 30mm

Arsenal

FDA UDI
ALPHATEC SPINE, INC.·00190376077536·Polyaxial Reduction Screw, 7.2 mm x 30 mm

Genius Total Knee System

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215023041·

Arsenal

FDA UDI
ALPHATEC SPINE, INC.·00844856086715·POLYAXIAL REDUCTION SCREW, 7.2mm X 30mm

Arsenal

FDA UDI
ALPHATEC SPINE, INC.·00190376074078·Polyaxial Screw, 7.2 mm x 30 mm

3.5 Driver Q Tip

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215061692·

PORTABLE INTENSIVE CARE UNIT

FDA 510(k)
FDA Class 3 ·Cardiovascular

OMNI-TRAK 3150/3155A SERIES MONITOR WITH ANESTHETIC AGENT, MODEL 3155A SERIES

FDA 510(k)
FDA Class 2 ·Cardiovascular

PEN NDL 32G 4MM PRO 14 BAG 700 CASE JPX

FDA Adverse Event
Malfunction ·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·March 11, 2025

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 22, 2013

ZOOM CRITICAL CARE BED

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FNL·April 19, 2011

ATTAIN OTW

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWP·July 10, 2008

BD SYRINGE 3ML LL 200 S/C

FDA Adverse Event
Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·December 12, 2025